Anti-Tmem27 antibody [EPR17748]
- RabMAb
- Recombinant
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(2 Publications)
Rabbit Recombinant Monoclonal Tmem27 antibody. Suitable for WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Mouse, Rat, Human samples. Cited in 2 publications.
View Alternative Names
TMEM27, UNQ679/PRO1312, CLTRN, Collectrin, Transmembrane protein 27
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tmem27 antibody [EPR17748] (AB200664)
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling Tmem27 with ab200664 at 1/10000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution.
Luminal surface and cytoplasm staining on Human kidney tissue is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Tmem27 antibody [EPR17748] (AB200664)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized BxPC-3 (Human pancreas adenocarcinoma cells) cells labeling Tmem27 with ab200664 at 1/500 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green).
Cytoplasm staining on BxPC-3 cell line is observed.
The nuclear counter stain is DAPI (blue).
Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows :
-ve control 1 : ab200664 at 1/500 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Tmem27 antibody [EPR17748] (AB200664)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HEK293 (Human embryonic kidney) cells labeling Tmem27 with ab200664 at 1/500 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green).
Cytoplasm staining on HEK293 cell line is observed.
The nuclear counter stain is DAPI (blue).
Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows :
-ve control 1 : ab200664 at 1/500 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tmem27 antibody [EPR17748] (AB200664)
Immunohistochemical analysis of paraffin-embedded Human cerebral cortex tissue labeling Tmem27 with ab200664 at 1/10000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution.
No staining on Human cerebral cortex tissue is observed (Negative control for Tmem27).
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Tmem27 antibody [EPR17748] (AB200664)
Intracellular flow cytometric analysis of 2% paraformaldehyde-fixed BxPC-3 (Human pancreas adenocarcinoma cells) cells labeling Tmem27 with ab200664 at 1/100 dilution (red) compared with a rabbit monoclonal IgG isotype control (ab172730;black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody; blue). Goat anti rabbit IgG (FITC) at 1/150 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tmem27 antibody [EPR17748] (AB200664)
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling Tmem27 with ab200664 at 1/10000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution.
Luminal surface and cytoplasm staining on rat kidney tissue is observed.
Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- WB
Supplier Data
Western blot - Anti-Tmem27 antibody [EPR17748] (AB200664)
The observed MW is consistent with what has been described in the literature PMID : 16330323.
Please note lanes 2-4 are negative controls for Tmem27.
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Tmem27 antibody [EPR17748] (ab200664) at 1/1000 dilution
Lane 1:
Human pancreas lysate at 10 µg
Lane 2:
Human fetal brain lysate at 10 µg
Lane 3:
Human fetal heart lysate at 10 µg
Lane 4:
Human fetal spleen lysate at 10 µg
Secondary
All lanes:
Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 25 kDa
Observed band size: 38 kDa
false
Exposure time: 3min
- WB
Unknown
Western blot - Anti-Tmem27 antibody [EPR17748] (AB200664)
The observed MW is consistent with what has been described in the literature PMID : 16330323.
Please note lanes 2-4 are negative controls for Tmem27.
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Tmem27 antibody [EPR17748] (ab200664) at 1/1000 dilution
Lane 1:
Human fetal kidney lysate at 10 µg
Lane 2:
Human fetal brain lysate at 10 µg
Lane 3:
Human fetal heart lysate at 10 µg
Lane 4:
Human fetal spleen lysate at 10 µg
Secondary
All lanes:
Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 19 kDa,25 kDa
Observed band size: 17 kDa,38 kDa
false
Exposure time: 5s
- WB
Supplier Data
Western blot - Anti-Tmem27 antibody [EPR17748] (AB200664)
The observed MW is consistent with what has been described in the literature PMID : 16330323.
Please note lanes 2-4 and 6-8 are negative controls for Tmem27.
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Tmem27 antibody [EPR17748] (ab200664) at 1/1000 dilution
Lane 1:
Mouse kidney lysate at 10 µg
Lane 2:
Mouse brain lysate at 10 µg
Lane 3:
Mouse heart lysate at 10 µg
Lane 4:
Mouse spleen lysate at 10 µg
Lane 5:
Rat kidney lysate at 10 µg
Lane 6:
Rat brain lysate at 10 µg
Lane 7:
Rat heart lysate at 10 µg
Lane 8:
Rat spleen lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 25 kDa
Observed band size: 38 kDa
false
Exposure time: 5s
Related conjugates and formulations (1)
-
Anti-Tmem27 antibody [EPR17748] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The involvement of Tmem27 extends to the regulation of amino acid transport and insulin exocytosis. It associates with the γ-aminobutyric acid type B receptor (GABBR) complex contributing to the modulation of nutrient uptake. Tmem27 influences the processing and trafficking of small neutral amino acids enhancing their absorption across epithelial barriers which is important for maintaining cellular homeostasis and metabolic activities.
Pathways
The function of Tmem27 is significant in the renin-angiotensin system and the insulin signaling pathway. In the renin-angiotensin system Tmem27 operates alongside the angiotensin-converting enzyme (ACE) to precisely regulate blood pressure homeostasis. It also acts within the insulin signaling pathway by modulating insulin secretion potentially working closely with glucose transporter type 4 (GLUT4) to ensure efficient glucose uptake by cells.
Product protocols
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Target data
Publications (2)
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The Journal of biological chemistry 298:102585 PubMed36223838
2022
Applications
Unspecified application
Species
Unspecified reactive species
Anticancer research 38:5217-5222 PubMed30194170
2018
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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